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Article

A novel mutation in K6b in pachyonychia congenita type 2.

The Journal of investigative dermatology - 1 Aug 2007

Sharma Vishakha M, Stein Sarah L

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 17429440
DOI: 10.1038/sj.jid.5700814

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A novel mutation in K6b in pachyonychia congenita type 2.PMID 17429440Read ↗

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Novel and recurrent keratin 6A (KRT6A) mutations in Chinese patients with pachyonychia congenita type 1.Semantic proximity Read ↗

[Pachyonychia congenita type 2 due to mutation in the keratin 6b gene].Semantic proximity Read ↗

Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.Semantic proximity Read ↗

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Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families.Semantic proximity Read ↗

Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.Semantic proximity Read ↗

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